- Trials with a EudraCT protocol (2,820)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,820 result(s) found.
Displaying page 81 of 141.
| EudraCT Number: 2020-004102-63 | Sponsor Protocol Number: CNS-Lymphoma-Vorax-1 | Start Date*: 2021-05-07 |
| Sponsor Name:Charité Universitätsmedizin Berlin | ||
| Full Title: AN OPEN LABEL, PHASE I/II STUDY TO INVESTIGATE THE USE OF VORAXAZE™ AS INTENDED INTERVENTION IN PATIENTS WITH CENTRAL NERVOUS SYSTEM LYMPHOMA AND WITH IMPAIRED RENAL FUNCTION BEING TREATED WITH HIG... | ||
| Medical condition: CNS lymphoma (CNSL) being treated with HD-MTX in patients with impaired renal function | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001366-38 | Sponsor Protocol Number: CCTU0263 | Start Date*: 2022-10-13 | |||||||||||
| Sponsor Name:Region Skåne – Skåne University Hospital | |||||||||||||
| Full Title: STEM-PD trial: A multicentre, single arm, first in human, dose-escalation trial, investigating the safety and tolerability of intraputamenal transplantation of human embryonic stem cell derived dop... | |||||||||||||
| Medical condition: Parkinson’s disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000547-24 | Sponsor Protocol Number: CCRG11-001 | Start Date*: 2012-02-27 | ||||||||||||||||
| Sponsor Name:Antwerp University Hospital | ||||||||||||||||||
| Full Title: Therapeutic efficacy of Wilms' tumor gene (WT1) mRNA-electroporated autologous dendritic cell vaccination in patients with solid tumors: a phase I/feasibility study | ||||||||||||||||||
| Medical condition: Therapeutic vaccination with dendritic cells loaded with Wilms' tumor 1 protein in patients with solid tumors | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-000714-33 | Sponsor Protocol Number: PT26/17/01 | Start Date*: 2023-02-21 | |||||||||||
| Sponsor Name:tiakis Biotech AG (formerly Proteo Biotech AG) | |||||||||||||
| Full Title: Efficacy and safety of Tiprelestat for treatment of severe COVID-19 (COMCOVID trial) | |||||||||||||
| Medical condition: Adult patients with COVID-19 fulfilling the following criteria: -First laboratory-confirmation of the current episode of SARS-CoV-2 infection (COVID-19) as determined by PCR or antigen test (no sel... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005575-13 | Sponsor Protocol Number: CMV12/12 | Start Date*: 2013-05-16 | ||||||||||||||||||||||||||
| Sponsor Name:Antwerp University Hospital | ||||||||||||||||||||||||||||
| Full Title: Prophylactic vaccination with autologous dendritic cells against human cytomegalovirus: a pilot study in patients awaiting kidney transplantation | ||||||||||||||||||||||||||||
| Medical condition: Cytomegalovirus infection in patients awaiting kidney transplantation and after kidney transplantation | ||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2022-002412-23 | Sponsor Protocol Number: DUO2022_01 | Start Date*: 2022-12-30 |
| Sponsor Name:MB PHARMA s. r. o. | ||
| Full Title: A prospective, randomized, double-blind, placebo-controlled Phase I/IIA Clinical Trial to demonstrate the safety and efficacy of DUOFAG® in bacterial infection treatment in patients with surgical w... | ||
| Medical condition: Bacterial infection with Staphylococcus aureus and/or Pseudomonas aeruginosa in the surgical wound. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-001693-33 | Sponsor Protocol Number: ITL-2002-CL-001 | Start Date*: 2022-03-30 | |||||||||||
| Sponsor Name:Intellia Therapeutics, Inc. | |||||||||||||
| Full Title: Phase 1/2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NTLA-2002 in Adults with Hereditary Angioedema (HAE) | |||||||||||||
| Medical condition: Hereditary Angioedema | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Trial now transitioned) FR (Trial now transitioned) DE (Trial now transitioned) ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004544-28 | Sponsor Protocol Number: MK-3475-04A | Start Date*: 2022-10-21 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
| Full Title: A Phase 1/2 Open-Label Rolling-Arm Umbrella Platform Study of Investigational Agents With or Without Pembrolizumab in Participants with PD-1/L1 Refractory Locally Advanced or Metastatic Urothelial ... | |||||||||||||
| Medical condition: Locally advanced or metastatic urothelial cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Temporarily Halted) DK (Trial now transitioned) IT (Trial now transitioned) NL (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002927-13 | Sponsor Protocol Number: FIL_A-BEGEV | Start Date*: 2022-03-22 | |||||||||||
| Sponsor Name:FONDAZIONE ITALIANA LINFOMI ONLUS | |||||||||||||
| Full Title: A phase I/II b (randomized controlled) study of atezolizumab combined to BEGEV regimen as first salvage treatment in patients with relapsed or refractory Hodgkin’s lymphoma candidate to autologous ... | |||||||||||||
| Medical condition: Refractory/relapsed Hodgkin Lymphoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-000715-25 | Sponsor Protocol Number: M15-340 | Start Date*: 2019-04-16 | |||||||||||
| Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
| Full Title: An Open-Label Multiple-Dose Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Upadacitinib in Pediatric Subjects with Polyarticular Course Juvenile Idiopathic Arthritis | |||||||||||||
| Medical condition: Polyarticular Course Juvenile Idiopathic Arthritis | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) ES (Restarted) IT (Trial now transitioned) SE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-001092-14 | Sponsor Protocol Number: TIGEM5_USH | Start Date*: 2023-10-12 | ||||||||||||||||
| Sponsor Name:FONDAZIONE TELETHON | ||||||||||||||||||
| Full Title: A phase I/II open label, dose escalation study of sub-retinal administration of a “mixture of two adeno-associated viral vectors of serotype 8 containing the 5 ´- half sequence of the human MYO7A ... | ||||||||||||||||||
| Medical condition: Usher syndrome (USH) is characterized by the association of sensorineural hearing loss, Retinitis Pigmentosa (RP), and, in some cases, vestibular dysfunction. It is the most frequent cause of deaf-... | ||||||||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2018-003047-32 | Sponsor Protocol Number: IRFMN-7557 | Start Date*: 2021-01-21 | |||||||||||
| Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
| Full Title: CardioPulmonary resuscitation with Argon (CPAr) trial | |||||||||||||
| Medical condition: Cardiac Arrest | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-004490-10 | Sponsor Protocol Number: 2012_32 | Start Date*: 2013-09-18 | |||||||||||
| Sponsor Name:Ghent University Hospital | |||||||||||||
| Full Title: A Multicenter Open label Phase 2 study of Carfilzomib Weekly plus Melphalan and Prednisone in Untreated Symptomatic Elderly Multiple Myeloma. | |||||||||||||
| Medical condition: A Multicenter Open label Phase 2 study of Carfilzomib Weekly plus Melphalan and Prednisone in Untreated Symptomatic Elderly Multiple Myeloma. | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002604-12 | Sponsor Protocol Number: PSY-NIL-0010 | Start Date*: 2022-02-09 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Unraveling the aesthetic mind in anhedonia, insights from pharmacological imaging of the human brain: A single-blind, randomized, placebo-controlled cross-over study | ||
| Medical condition: Depression | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001730-34 | Sponsor Protocol Number: TX200-KT02 | Start Date*: 2020-03-24 | |||||||||||
| Sponsor Name:Sangamo Therapeutics France SAS | |||||||||||||
| Full Title: A Multicentre, Open-Label, Single Ascending Dose, Dose-Ranging, Phase I/IIa Study to Evaluate the Safety and Tolerability of an Autologous Antigen-Specific Chimeric Antigen Receptor T Regulatory Ce... | |||||||||||||
| Medical condition: Prevention of immune mediated allograft rejection in patients with end-stage renal disease (ESRD) who are tissue typed as HLA-A*02 negative and have received a kidney transplant from an HLA-A*02 po... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) NL (Trial now transitioned) DE (Completed) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000588-53 | Sponsor Protocol Number: SNIPER | Start Date*: 2023-02-07 | |||||||||||
| Sponsor Name:RIGENERAND Srl | |||||||||||||
| Full Title: RR001 in combination with chemotherapy for patients with locally advanced pancreatic adenocarcinoma: open-label, non-randomized dose escalation phase I/IIa study | |||||||||||||
| Medical condition: Locally advanced pancreatic adenocarcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-001855-22 | Sponsor Protocol Number: M14AFS | Start Date*: 2015-01-14 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Netherlands Cancer Institute- Antoni van Leeuwenhoek Hospital | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Phase I/II study with the combination of afatinib and selumetinib in advanced KRAS mutant positive and PIK3CA wildtype non-small cell lung cancer and colorectal cancer | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Patients with histological or cytological proof of advanced KRAS mutant and PIK3CA wildtype non small cell lung cancer (NSCLC) and colorectal cancer (CRC). In part B: for which first-line treatment... | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-002017-22 | Sponsor Protocol Number: 63723283LUC1001 | Start Date*: 2016-11-16 | |||||||||||
| Sponsor Name:Janssen-Cilag International NV | |||||||||||||
| Full Title: A First-in-Human, Open-label, Phase 1/2 Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of JNJ-63723283, an Anti-PD-1 Monoclonal Antibody, in Subjects with A... | |||||||||||||
| Medical condition: Advanced Stage Solid Tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) PL (Trial now transitioned) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-002211-11 | Sponsor Protocol Number: MIP-IB12 | Start Date*: 2008-02-13 | |||||||||||
| Sponsor Name:Molecular Insight Pharmaceuticals, Inc | |||||||||||||
| Full Title: A PHASE I-II STUDY EVALUATING THE MAXIMUM TOLERATED DOSE, DOSIMETRY, SAFETY, AND EFFICACY OF ULTRATRACE™ IOBENGUANE I 131 IN PATIENTS WITH MALIGNANT PHEOCHROMOCYTOMA/PARAGANGLIOMA | |||||||||||||
| Medical condition: MALIGNANT PHEOCHROMOCYTOMA/PARAGANGLIOMA | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-001555-14 | Sponsor Protocol Number: NBK272/1/2021 | Start Date*: 2023-01-05 |
| Sponsor Name:Medical University of Gdańsk | ||
| Full Title: Assessment of the effect of Wharton's jelly mesenchymal stem cell preparation (WJMSCs) in the treatment of fibrotic interstitial lung diseases | ||
| Medical condition: fibrotic interstitial lung disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: PL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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